Optically similar reference samples

• US 7,202,091 B2
• Filed: 10/28/2002
• Issued: 04/10/2007
• Est. Priority Date: 04/11/2001
• Status: Expired due to Fees

• Current Assignee: Inlight Solutions, Inc.
• Original Assignee: Inlight Solutions, Inc.
• Inventors: Johnson, Robert D., Hull, Edward L., Jones, Howland D. T., Vanslyke, Stephen J., Nunez, David J.
• Primary Examiner(s): WALLENHORST, MAUREEN
• Application Number:
  US10/281,576
• Publication Number:
  US 20040082070A1
• Time in Patent Office: 1,625 Days
• Field of Search: 436/8, 436/19, 436164-166, 252/408.1, 356/300, 356/317, 356/51, 422/82.05, 422/82.09, 600/476, 600/310, 600/473
• US Class Current: 436/164
• CPC Class Codes: A61B 5/0075 by spectroscopy, i.e. measuring spectra, e.g. Raman spectroscopy, infrared absorption spectroscopy A61B5/0071 takes precedence
• CPC Class Codes: G01J 3/02 Details
• CPC Class Codes: G01J 3/0216 using light concentrators or collectors or condensers
• CPC Class Codes: G01J 3/0218 using optical fibers
• CPC Class Codes: G01J 3/10 Arrangements of light sources specially adapted for spectrometry or colorimetry
• CPC Class Codes: G01N 21/278 Constitution of standards
• CPC Class Codes: G01N 21/4785 Standardising light scatter apparatus; Standards therefor
• CPC Class Codes: G01N 21/49 within a body or fluid
• CPC Class Codes: G01N 2201/1293 resolving multicomponent spectra
• CPC Class Codes: Y10T 436/10 Composition for standardization, calibration, simulation, stabilization, preparation or preservation; processes of use in preparation for chemical testing

Abstract

Systems and methods for establishing and/or maintaining the accuracy of a multivariate calibration model designed for quantitative optical spectroscopic measurement of attributes or analytes in bodily tissues, bodily fluids or other biological samples, which are particularly useful when the spectral absorbance of the attribute or analyte is small relative to the background. The present invention provides an optically similar reference sample to reduce the effect of instrument or environment variation on the measurement capability of the model. The optically similar reference can be a gel composition having scattering particles suspended therein. The reference gel can be directly applied to a spectroscopic instrument sampler, or can be in a container specifically designed for optimal coupling to a spectroscopic instrument.

Claims

1. A method of characterizing the performance of an infrared spectroscopic system, comprising:

a. providing a reference sample comprising a gelling agent;

a scattering agent that scatters infrared energy; and

water;

b. using the infrared spectroscopic system to measure the response of the reference sample to incident radiation;

c. characterizing the performance of the infrared spectroscopic system from a comparison of the measured response with a response expected from the known properties of the reference sample.

2. A method as in claim 1, wherein the scattering agent comprises a mesh, a filament, or a combination thereof.

3. A method as in claim 1, wherein the gelling agent comprises hydroxyethylcellulose.

4. A method as in claim 3, wherein the hydroxyethylcellulose (HEC) and the water are present at a ratio of 30 weight % HEC to 70 weight % water.

5. A method as in claim 1, wherein the gelling agent comprises polyvinyl alcohol.

6. A method as in claim 5, wherein the polyvinyl alcohol (PVA) and the water are present at a ratio of 30 weight % PVA to 70 weight % water.

7. A method as in claim 1, wherein the gelling agent comprises an initiator and a crosslinking agent that contains a plurality of vinyl groups.

8. A method as in claim 7, wherein the crosslinking agent comprises N,N′

-methylenebisacrylamide, ethylene glycol dimethacrylate, bisacrylamide, or a combination thereof.

9. A method as in claim 7, wherein the initiator comprises a peroxide, benzoyl peroxide, a persulfate, ammonium persulfate, azobisisobutyronitrile, a photochemically activated initiator, methylene blue, riboflavin, ammonium persulfate in the presence of N,N,N′

,N′

-Tetramethylethylenediamine, or a combination thereof.

10. A method as in claim 7, wherein the gelling agent further comprises a monomer that contains a vinyl group.

11. A method as in claim 10, wherein the monomer comprises acrylamide, 2-hydroxyethyl methacrylate, poly(ethylene glycol) methacrylate, 1-vinyl-2-pyrrolidinone, or a combination thereof.

12. A method as in claim 1, wherein the reference sample further comprises an analyte.

13. A method as in claim 1, wherein the reference sample further comprises a protein, a lipid, or a combination thereof.

14. A method as in claim 1, wherein the reference sample further comprises a temperature control agent, a pH control agent, an ionic control agent, or a combination thereof.

15. A method as in claim 1, wherein the scattering agent comprises a first plurality of scattering particles having a first scattering characteristic and a second plurality of scattering particles having a second scattering characteristic, wherein the first scattering characteristic is different than the second scattering characteristic.

16. A method as in claim 1, wherein the scattering agent comprises particles of at least two different sizes.

17. A method as in claim 1, wherein the scattering agent comprises particles of at least two different shapes.

18. A method as in claim 1, wherein the scattering agent comprises particles of at least two different refractive indices.

19. A method as in claim 1, wherein the scattering agent comprises polystyrene particles.

20. A method as in claim 19, wherein the polystyrene particles have a diameter chosen from the group consisting of:

0.2 to 4 μ

m;

0.14 to 0.35 μ

m;

0.3 μ

m;

0.8 to 1 μ

m;

0.9 to 0.95 μ

m;

0.93 μ

m;

5 to 6 μ

m;

4 to 5 μ

m;

5.3 to 5.7 μ

m;

5.5 μ

m;

6 to 7 μ

m;

6.2 to 6.5 μ

m; and

6.3 μ

m.

21. A method as in claim 19, where the polystyrene particles have a diameter of 0.8 to 1.0 μ

m, and wherein the polystyrene particles are present at a concentration chosen from the group consisting of;

1400 to 1800 mg/dL; and

1600 mg/dL.

22. A method as in claim 21, wherein the reference sample comprises:

a. 1,400 to 1,800 mg/dL polystyrene beads;

b. 500 to 1,500 mg/dL viscosity control agent; and

c. 75,000 to 80,000 mg/dL water.

23. A method as in claim 22, wherein the reference sample has a spectral absorbance peak at a wavelength of 5,200 cm-1 and 6,900 cm-1.

24. A method as in claim 21, wherein the reference sample comprises:

a. 1,600 mg/dL polystyrene beads;

b. 1000 mg/dL viscosity control agent; and

c. 77,000 mg/dL water.

25. A method as in claim 19, wherein the polystyrene particles comprise a first group of polystyrene particles having a first diameter and a second group of polystyrene particles having a second diameter wherein the first diameter is different than the second diameter.

26. A method as in claim 25, further comprising a third group of polystyrene particles having a third diameter wherein the third diameter is different than the first and the second diameter.

27. A method as in claim 26, further comprising a fourth group of polystyrene particles having a fourth diameter wherein the fourth diameter is different from the first, second and third diameter.

28. A method as in claim 27, wherein the first diameter is 0.25 to 0.35 μ

m, the second diameter is 0.9 to 0.95 μ

m, the third diameter is 5.3 to 5.7 μ

m, and the fourth diameter is 6.2 to 6.5 μ

m.

29. A method as in claim 28, wherein the first diameter is 0.3 μ

m, the second diameter is 0.93 μ

m, the third diameter is 5.5 μ

m and the fourth diameter is 6.3μ

m.

30. A method as in claim 28, wherein the reference sample comprises:

a. 150 to 250 mg/dL of the first group of polystyrene beads;

b. 900 to 950 mg/dL of the second group of polystyrene beads;

c. 50 to 350 mg/dL of the third group of polystyrene beads; and

d. 250 to 700 mg/dL of the fourth group of polystyrene beads.

31. A method as in claim 30, wherein the reference comprises:

a. 1,300 to 2,300 mg/dL polystyrene beads;

b. 1,000 to 4,000 mg/dL viscosity control agent; and

c. 70,000 to 80,000 mg/dL water.

32. A method as in claim 31, wherein the reference sample has a spectral absorbance peak at a wavelength of 5,200 cm-1 and 6,900 cm-1.

33. A method as in claim 28, wherein the reference sample comprises:

a. 170 mg/dL of the first group of polystyrene beads;

b. 940 mg/dL of the second group of polystyrene beads;

c. 310 mg/dL of the third group of polystyrene beads; and

d. 300 mg/dL of the fourth group of polystyrene beads.

34. A method as in claim 33, wherein the reference samole comprises:

a. 1,700 mg/dL polystyrene beads;

b. 1,000 mg/dL viscosity control agent; and

c. 75,000 mg/dL water.

35. A method as in claim 33, wherein the reference sample comprises:

a. 1,850 mg/dL polystyrene beads;

b. 4,000 mg/dL viscosity control agent; and

c. 70,000 mg/dL water.

36. A method as in claim 28, wherein the reference sample comprises:

a. 200 mg/dL of the first group of polystyrene beads;

b. 920 mg/dL of the second group of polystyrene beads;

c. 90 mg/dL of the third group of polystyrene beads; and

d. 640 mg/dL of the fourth group of polystyrene beads.

37. A method as in claim 1, wherein the reference sample further comprises a viscosity control agent.

38. A method as in claim 37, wherein the viscosity control agent comprises sodium lauryl sulfate, ammonium lauryl sulfate, or combinations thereof.

39. A method as in claim 37, wherein the viscosity control agent comprises sodium lauryl sulfate, ammonium lauryl sulfate, a latex emulsion, a cellulosic water-soluble polymer, a water-soluble resin, a natural gum, a preservative, a surfactant, a defoamer, a plasticizer, an organic solvent, or combinations thereof.

40. A method as in claim 37, wherein the reference sample comprises:

a. 30,000–

40,000 mg/dL gelling agent;

b. 1,000–

2,500 mg/dL polystyrene particles;

c. 100–

5.000 mg/dL viscosity control agent; and

d. 60,000–

85,000 mg/dL water.

41. A method as in claim 1, wherein the reference sample has spectral absorbance peaks at wavelengths of about 5,200 cm-1 and about 6,900 cm-1.

42. A method as in claim 1, wherein the gelling agent contains a plurality of vinyl groups;

and wherein the reference sample further comprises an initiator.

43. A method as in claim 42, wherein the gelling agent comprises N,N′

-methylenebisacrylamide, ethylene glycol dimethacrylate, bisacrylamide, or a combination thereof.

44. A method as in claim 42, wherein the initiator comprises peroxide, benzoyl peroxide, a persulfate, ammonium persulfate, azobisisobutyronitrile, a photochemically activated initiator, methylene blue, riboflavin, ammonium persulfate in the presence of N,N,N′

, N′

-Tetramethylethylenediamine, or a combination thereof.

45. A method as in claim 42, wherein the reference sample further comprises a monomer that contains a vinyl group.

46. A method as in claim 45, wherein the monomer comprises acrylamide, 2-hydroxyethyl methacrylate, poly(ethylene glycol) methacrylate, 1-vinyl-2-pyrrolidinone, or a combination thereof.

47. A method as in claim 42, wherein the reference sample further comprises an accelerant.